Back to Search
Start Over
Dysregulated signaling hubs of liver lipid metabolism reveal hepatocellular carcinoma pathogenesis.
- Source :
-
Nucleic acids research [Nucleic Acids Res] 2016 Jul 08; Vol. 44 (12), pp. 5529-39. Date of Electronic Publication: 2016 May 23. - Publication Year :
- 2016
-
Abstract
- Hepatocellular carcinoma (HCC) has a high mortality rate and early detection of HCC is crucial for the application of effective treatment strategies. HCC is typically caused by either viral hepatitis infection or by fatty liver disease. To diagnose and treat HCC it is necessary to elucidate the underlying molecular mechanisms. As a major cause for development of HCC is fatty liver disease, we here investigated anomalies in regulation of lipid metabolism in the liver. We applied a tailored network-based approach to identify signaling hubs associated with regulation of this part of metabolism. Using transcriptomics data of HCC patients, we identified significant dysregulated expressions of lipid-regulated genes, across many different lipid metabolic pathways. Our findings, however, show that viral hepatitis causes HCC by a distinct mechanism, less likely involving lipid anomalies. Based on our analysis we suggest signaling hub genes governing overall catabolic or anabolic pathways, as novel drug targets for treatment of HCC that involves lipid anomalies.<br /> (© The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.)
- Subjects :
- Carcinoma, Hepatocellular metabolism
Carcinoma, Hepatocellular pathology
Gene Expression Regulation, Neoplastic genetics
Humans
Liver metabolism
Liver pathology
Liver Neoplasms metabolism
Liver Neoplasms pathology
Transcriptome genetics
Carcinoma, Hepatocellular genetics
Lipid Metabolism genetics
Liver Neoplasms genetics
Metabolic Networks and Pathways genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1362-4962
- Volume :
- 44
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Nucleic acids research
- Publication Type :
- Academic Journal
- Accession number :
- 27216817
- Full Text :
- https://doi.org/10.1093/nar/gkw462